Does HUMAN RHO IMMUNE GLOBULIN Cause Syringe issue? 154 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 154 reports of Syringe issue have been filed in association with HUMAN RHO IMMUNE GLOBULIN (RhoGAM Ultra-Filtered PLUS). This represents 12.8% of all adverse event reports for HUMAN RHO IMMUNE GLOBULIN.
154
Reports of Syringe issue with HUMAN RHO IMMUNE GLOBULIN
12.8%
of all HUMAN RHO IMMUNE GLOBULIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Syringe issue From HUMAN RHO IMMUNE GLOBULIN?
Of the 154 reports, 1 (0.6%) required hospitalization.
Is Syringe issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HUMAN RHO IMMUNE GLOBULIN. However, 154 reports have been filed with the FAERS database.
What Other Side Effects Does HUMAN RHO IMMUNE GLOBULIN Cause?
No adverse event (238)
Drug ineffective (201)
Device issue (167)
Nausea (111)
Treatment failure (110)
Arthralgia (109)
Therapy non-responder (107)
Pain in extremity (104)
Therapeutic product effect decreased (104)
Joint swelling (100)
What Other Drugs Cause Syringe issue?
LEUPROLIDE (7,847)
USTEKINUMAB (2,169)
DEVICE (634)
OCTREOTIDE (621)
RISPERIDONE (540)
GUSELKUMAB (458)
MEDROXYPROGESTERONE (354)
PALIPERIDONE (299)
GOLIMUMAB (269)
OMALIZUMAB (257)
Which HUMAN RHO IMMUNE GLOBULIN Alternatives Have Lower Syringe issue Risk?
HUMAN RHO IMMUNE GLOBULIN vs HUMIRA
HUMAN RHO IMMUNE GLOBULIN vs HUMIRA PEN
HUMAN RHO IMMUNE GLOBULIN vs HYALURONATE
HUMAN RHO IMMUNE GLOBULIN vs HYALURONIC ACID
HUMAN RHO IMMUNE GLOBULIN vs HYALURONIC ACID\LIDOCAINE